Clinical Research Nurse - Mercy Springfield

Mercy • Springfield, MO

9d • Onsite

About The Position

The Clinical Research Nurse (CRN) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. Duties also include the collection, compilation, documentation and analysis of clinical research data while following local, state and federal regulations. The Clinical Research Nurse will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse will assist with communication and relationship building with sponsors and CROs. Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards. Position Details: Clinical Research Registered Nurse (RN) Position Summary The Clinical Research RN coordinates and conducts clinical trial activities while ensuring participant safety, protocol compliance, and accurate data collection. This role works closely with investigators, sponsors, and study participants to support successful research outcomes.

Requirements

• Nursing Diploma, ADN, or BSN.
• Current RN license in the state of practice.
• BSN: 2+ years of nursing experience.
• ADN/Diploma: 3+ years of nursing experience.
• Experience performing patient assessments, vital signs, ECGs, spirometry, phlebotomy, or willingness to learn.
• Strong communication, organizational, and problem-solving skills.
• Proficiency with Microsoft Office and computer applications.

Nice To Haves

• 2+ years of clinical research experience.
• Phlebotomy experience.
• Knowledge of clinical trial protocols, GCP, and regulatory requirements.

Responsibilities

• Coordinate clinical research activities and patient visits.
• Screen, consent, educate, and monitor study participants.
• Administer investigational products and perform protocol-required procedures.
• Ensure compliance with study protocols, GCP, and regulatory requirements.
• Collect, document, and maintain accurate study data and source records.
• Process laboratory specimens and maintain study supplies.
• Monitor participant safety and report adverse events as required.
• Collaborate with investigators, sponsors, CROs, and research staff.
• Support patient recruitment efforts and community outreach activities.
• Assist with training and mentoring research team members.
• Attend study meetings and perform other duties as assigned.

Benefits

• medical coverage
• dental coverage
• vision coverage
• paid time off
• tuition support
• matched retirement plans

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree